Abstract

Polycyclic aromatic hydrocarbons (PAHs) are compounds that can be quantified by fluorescence due to their high quantum yield. Haloalkalitolerant bacteria tolerate wide concentration ranges of NaCl and pH. They are potentially useful in the PAHs bioremediation of saline environments. However, it is known that salinity of the sample affects fluorescence signal regardless of the method. The objective of this work was to carry out a comparative study based on the sensitivity, linearity, and detection limits of the excitation, emission, and synchronous fluorescence methods, during the quantification of the residual anthracene concentration from the following haloalkalitolerant actinomycetes cultures Kocuria rosea, Kocuria palustris, Microbacterium testaceum, and 4 strains of Nocardia farcinica, in order to establish the proper fluorescence method to study the PAHs biodegrading capacity of haloalkalitolerant actinobacteria. The study demonstrated statistical differences among the strains and among the fluorescence methods regarding the anthracene residual concentration. The results showed that excitation and emission fluorescence methods performed very similarly but sensitivity in excitation fluorescence is slightly higher. Synchronous fluorescence using Δλ = 150 nm is not the most convenient method. Therefore we propose the excitation fluorescence as the fluorescence method to be used in the study of the PAHs biodegrading capacity of haloalkalitolerant actinomycetes.

Highlights

  • Polycyclic aromatic hydrocarbons (PAHs) are a group of highly toxic and persistent organic pollutants that are widely distributed in the environment worldwide [1]

  • Fluorescence is a very convenient method to study PAHs biodegradation because it is simple, easy, fast, inexpensive, very sensitive, and reproducible. For these reasons fluorescence was our method of choice for studying the capabilities of haloalkalitolerant actinomycetes for degrading PAHs

  • These bacteria require NaCl for growing; our study was focussed to investigate the performance of excitation, emission, and synchronous fluorescence in the determination of anthracene in the presence of different NaCl concentrations in order to stablish the most proper fluorescence method to study the PAHs biodegrading properties of these bacteria

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Summary

Introduction

Polycyclic aromatic hydrocarbons (PAHs) are a group of highly toxic and persistent organic pollutants that are widely distributed in the environment worldwide [1]. PAHs are ubiquitous, very stable in the environment [2]. They are potentially dangerous due to their carcinogenicity and mutagenicity [3]; their removal is an issue of great interest. One of the compounds used as model in studies of PAHs degradation by microorganisms is anthracene, a polycyclic aromatic hydrocarbon of three rings, which has been listed as one of the priority environmental pollutants by the United States Environmental Protection Agency. Anthracene is usually used as a PAH model in studies of degradation [6,7,8]

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